SN1??Type Substitution Reactions of N??Protected β??Hydroxytyrosine Esters: Stereoselective Synthesis of β??Aryl and β??Alkyltyrosines
D Wilcke, E Herdtweck, T Bach
Index: Wilcke, David; Herdtweck, Eberhardt; Bach, Thorsten Chemistry - An Asian Journal, 2012 , vol. 7, # 6 p. 1372 - 1382
Full Text: HTML
Citation Number: 14
Abstract
Abstract The title compounds were prepared by aldol reaction of anisaldehyde and the respective N, N-dibenzyl glycinates. Deprotection of the nitrogen atom with Pearlman's catalyst delivered the unprotected β-hydroxytyrosine esters, which were further N-protected as N, N-phthaloyl (Phth) and N-fluorenylmethylcarbonyloxy (Fmoc) derivatives. The Friedel– Crafts reaction with various arenes was studied employing these alcohols as electrophiles ...
Related Articles:
[Jastrzebska; Derdowska; Kuncarowa; Slaninova; Lammek; Olejniczak; Zabrocki Polish Journal of Chemistry, 2002 , vol. 76, # 6 p. 823 - 830]
Specificity of creatine kinase. New glycocyamines and glycocyamine analogs related to creatine
[Rowley,G.L. et al. Journal of the American Chemical Society, 1971 , vol. 93, p. 5542 - 5551]